UQCRH

Gene

ubiquinol-cytochrome c reductase hinge protein

HGNCHGNC:12590 EnsemblENSG00000173660 NCBI Gene7388

Locus: gene with protein productLocation: 1p33

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asQCR6 · UQCR8

View full nomenclature history (3)

Alias symbolsQCR6, UQCR8

Alias namesubiquinol-cytochrome c reductase, complex III subunit VIII

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Congenital bilateral absence of vas deferens

Hirschsprung disease

Carcinoma, Hepatocellular

Neoplasms

Venous Thromboembolism

Alzheimer's Disease

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Mitochondrial complex III: ubiquinol-cytochrome c reductase complex subunits

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.

Open TargetsGene–disease associations from the Open Targets Platform.